Electroactivity of RuO2-IrO2 mixed nanocatalysts toward the oxygen evolution reaction in a water electrolyzer supplied by a solar profile

被引:160
作者
Audichon, Thomas [1 ]
Mayousse, Eric [2 ]
Morisset, Sophie [3 ]
Morais, Claudia [1 ]
Comminges, Clement [1 ]
Napporn, Teko W. [1 ]
Kokoh, K. Boniface [1 ]
机构
[1] Univ Poitiers, IC2MP UMR CNRS 7285, Equipe SAMCat, Dept Chim,TSA 51106, F-86073 Poitiers 09, France
[2] CEA, LITEN, DEHT, LCPEM, F-38054 Grenoble, France
[3] Univ Poitiers, IC2MP UMR CNRS 7285, PREMICAT, Dept Chim,TSA 51106, F-86073 Poitiers 09, France
关键词
Hydrogen production; Ruthenium-iridium oxide; Oxygen evolution reaction; Electrochemical impedance spectroscopy; Water electrolysis; CHARGE STORAGE MECHANISM; ELECTROCATALYTIC PERFORMANCE; HYDROGEN-PRODUCTION; RUTHENIUM DIOXIDE; RUO2; ELECTRODES; ACID-SOLUTIONS; IRIDIUM OXIDE; ENERGY-SYSTEM; SURFACE; TECHNOLOGIES;
D O I
10.1016/j.ijhydene.2014.07.170
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Pure crystalline ruthenium-iridium oxide materials were synthesized with high surface area by co-precipitation method in ethanol medium. Cyclic and linear scan voltammetries were then undertaken to evaluate the effect of mixing iridium and ruthenium oxides on the oxygen evolution reaction (OER). The activity of these anode catalysts was evidenced through the determination of their capacitances, surface charges and Tafel slopes. It was found that the Ru0.9Ir0.1O2 catalyst presented catalytic properties close to those of RuO2, in particular for low overpotentials. The proposed synthesis method was also shown to be suitable for recovering large catalyst amount for O-2 production in a large surface proton exchange membrane water electrolyzer (PEMWE). Polarization measurements were therefore performed in a single PEMWE cell and the durability of the catalytic materials was evaluated by supplying a solar power profile. The efficiency loss at 1 A cm(-2) and 80 degrees C was only 90 mu Vh(-1) for 1000 h under galvanodynamic operating conditions for Ru0.9Ir0.1O2 as anode, while the cell voltage varied between 1.75 and 1.85 V. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16785 / 16796
页数:12
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